Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methane → 7-Phenylacetamido-3-formyl-3-cephem-4-carboxylic acid benzhydrylester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methane | HCID 297 | — |
| 반응물 | Phenylacetyl chloride | HCID 7679 | — |
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | trimethylsilyl N-trimethylsilylethanimidate | HCID 25248 | — |
| 반응물 | 7-Amino-3-formyl-3-cephem-4-carboxylic acid | HCID 87203762 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 7-Phenylacetamido-3-formyl-3-cephem-4-carboxylic acid benzhydrylester | HCID 131721061 | — |
반응 단계
2.28 g of 7-amino-3-formyl-3-cephem-4-carboxylic acid are bisilylated as described in example 19 with 5.4 ml of N,O-bis-(trimethylsilyl)-acetamide, reacted with phenylacetic acid chloride, and then hydrolysed with 0.4 ml of water. The hydrolysed reaction mixture is treated with 1 g of activated charcoal and then filtered. The yellow filtrate is mixed with 20 ml of a 10% solution of diphenyldiazomethane in dichloromethane, and then concentrated to 10 ml in vacuo. The product is precipitated from the residue of evaporation thus obtained by adding 100 ml of n-hexane. 7-phenylacetamido-3-formyl-3-cephem-4-carboxylic acid benzhydrylester is thus obtained as a slightly yellowish product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06034237 |
| 출처 데이터셋 | uspto-grants-2000_03 |
| ORD ID | ord-db20c17a24f94f15a9c75db0555fc971 |
| 출처 메모 | uspto-grants-2000_03 |